日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high-risk lineage ambiguous leukemia

t(14;16)(q32;q24)导致的FOXF1/FENDRR基因失调定义了一种高危谱系模糊白血病亚型。

Di Giacomo, Danika; Pölönen, Petri; Bardelli, Valentina; Kimura, Shunsuke; Pierini, Valentina; Pagliaro, Luca; Arniani, Silvia; Chang, Yunchao; Gao, Qingsong; Montefiori, Lindsey E; Wu, Yiming; Park, Chun Shik; Wright, William C; Vento, Federica; Wei, Huimei; Matteucci, Caterina; Lei, Shaohua; Rosikiewicz, Wojciech; Nardelli, Carlotta; Lema Fernandez, Anair Graciela; Østergaard, Anna; Backhaus, Emily A; Baviskar, Pradyumna; Cerrano, Marco; Leoncin, Matteo; Manabe, Atsushi; Hirabayashi, Shinsuke; Takita, Junko; Hasegawa, Daisuke; Miyamoto, Satoshi; Macchiarulo, Antonio; Xu, Jason; Teachey, David Trent; Roti, Giovanni; Iacobucci, Ilaria; La Starza, Roberta; Mecucci, Cristina; Mullighan, Charles G

Tet2 deficiency promotes IgG1+ B-cell expansion and differentiation blockade through deregulation of the Nfkbia-c-Rel axis

Tet2 缺陷通过 Nfkbia-c-Rel 轴的失调促进 IgG1+ B 细胞扩增和分化阻滞

Ghamlouch, Hussein; Degaud, Michaël; Della-Valle, Veronique; Eeckhoutte, Alexandre; Armand, Marine; Joudat, Amina; Decaudin, Camille; Dominguez, Pilar M; Rosikiewicz, Wojciech; Pawlikowska, Patrycja; Darwiche, Walaa; Mouly, Enguerran; Li, Sheng; Melnick, Ari M; Aoufouchi, Said; Bernard, Olivier A

CTCF is selectively required for maintaining chromatin accessibility and gene expression in human erythropoiesis.

CTCF 是人类红细胞生成过程中维持染色质可及性和基因表达所必需的

Yang Xue, Cheng Li, Xin Ye, Zhang Jianxiang, Chen Xinfeng, Xu Jinchao, Zhang Mengli, Feng Ruopeng, Hyle Judith, Qi Wenjie, Rosikiewicz Wojciech, Xu Beisi, Li Chunliang, Xu Peng

Deciphering the role of RNA in regulating CTCF's DNA binding affinity in leukemia cells.

揭示 RNA 在调节白血病细胞中 CTCF DNA 结合亲和力中的作用

Hyle Judith, Qi Wenjie, Djekidel Mohamed Nadhir, Rosikiewicz Wojciech, Xu Beisi, Li Chunliang

Targeting DCAF5 suppresses SMARCB1-mutant cancer by stabilizing SWI/SNF

靶向DCAF5可通过稳定SWI/SNF抑制SMARCB1突变型癌症。

Sandi Radko-Juettner # ,Hong Yue # ,Jacquelyn A Myers ,Raymond D Carter ,Alexis N Robertson ,Priya Mittal ,Zhexin Zhu ,Baranda S Hansen ,Katherine A Donovan ,Moritz Hunkeler ,Wojciech Rosikiewicz ,Zhiping Wu ,Meghan G McReynolds ,Shourya S Roy Burman ,Anna M Schmoker ,Nada Mageed ,Scott A Brown ,Robert J Mobley ,Janet F Partridge ,Elizabeth A Stewart ,Shondra M Pruett-Miller ,Behnam Nabet ,Junmin Peng ,Nathanael S Gray ,Eric S Fischer ,Charles W M Roberts

Acute myeloid leukemias with UBTF tandem duplications are sensitive to menin inhibitors

具有 UBTF 串联重复的急性髓系白血病对 menin 抑制剂敏感

Juan M Barajas, Milad Rasouli, Masayuki Umeda, Ryan Hiltenbrand, Sherif Abdelhamed, Rebecca Mohnani, Bright Arthur, Tamara Westover, Melvin E Thomas 3rd, Minoo Ashtiani, Laura J Janke, Beisi Xu, Ti-Cheng Chang, Wojciech Rosikiewicz, Emily Xiong, Chandra Rolle, Jonathan Low, Reethu Krishan, Guangchun

Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement

DNA甲基化分析在遗传未明的儿童癫痫诊断中的应用及CHD2表观遗传特征的完善

LaFlamme, Christy W; Rastin, Cassandra; Sengupta, Soham; Pennington, Helen E; Russ-Hall, Sophie J; Schneider, Amy L; Bonkowski, Emily S; Almanza Fuerte, Edith P; Allan, Talia J; Zalusky, Miranda Perez-Galey; Goffena, Joy; Gibson, Sophia B; Nyaga, Denis M; Lieffering, Nico; Hebbar, Malavika; Walker, Emily V; Darnell, Daniel; Olsen, Scott R; Kolekar, Pandurang; Djekidel, Mohamed Nadhir; Rosikiewicz, Wojciech; McConkey, Haley; Kerkhof, Jennifer; Levy, Michael A; Relator, Raissa; Lev, Dorit; Lerman-Sagie, Tally; Park, Kristen L; Alders, Marielle; Cappuccio, Gerarda; Chatron, Nicolas; Demain, Leigh; Genevieve, David; Lesca, Gaetan; Roscioli, Tony; Sanlaville, Damien; Tedder, Matthew L; Gupta, Sachin; Jones, Elizabeth A; Weisz-Hubshman, Monika; Ketkar, Shamika; Dai, Hongzheng; Worley, Kim C; Rosenfeld, Jill A; Chao, Hsiao-Tuan; Neale, Geoffrey; Carvill, Gemma L; Wang, Zhaoming; Berkovic, Samuel F; Sadleir, Lynette G; Miller, Danny E; Scheffer, Ingrid E; Sadikovic, Bekim; Mefford, Heather C

PHF6 cooperates with SWI/SNF complexes to facilitate transcriptional progression

PHF6 与 SWI/SNF 复合物协同促进转录进程

Priya Mittal, Jacquelyn A Myers, Raymond D Carter, Sandi Radko-Juettner, Hayden A Malone, Wojciech Rosikiewicz, Alexis N Robertson, Zhexin Zhu, Ishwarya V Narayanan, Baranda S Hansen, Meadow Parrish, Natarajan V Bhanu, Robert J Mobley, Jerold E Rehg, Beisi Xu, Yiannis Drosos, Shondra M Pruett-Miller

Genomic and global gene expression profiling in pediatric and young adult acute leukemia with PICALM::MLLT10 Fusion

PICALM::MLLT10融合基因在儿童和青少年急性白血病中的基因组和全局基因表达谱分析

Ma, Jingqun; Liu, Yen-Chun; Voss, Rebecca K; Ma, Jing; Palagani, Ajay; Caldwell, Elizabeth; Rosikiewicz, Wojciech; Cardenas, Maria; Foy, Scott; Umeda, Masayuki; Wilkinson, Mark R; Inaba, Hiroto; Klco, Jeffery M; Rubnitz, Jeffrey E; Wang, Lu

Histone lysine demethylase 4 family proteins maintain the transcriptional program and adrenergic cellular state of MYCN-amplified neuroblastoma

组蛋白赖氨酸去甲基化酶 4 家族蛋白维持 MYCN 扩增神经母细胞瘤的转录程序和肾上腺素能细胞状态

Ahmed Abu-Zaid, Jie Fang, Hongjian Jin, Shivendra Singh, Prahalathan Pichavaram, Qiong Wu, Heather Tillman, Laura Janke, Wojciech Rosikiewicz, Beisi Xu, Lee-Ann Van De Velde, Yian Guo, Yimei Li, Noha A M Shendy, Ian M Delahunty, Zoran Rankovic, Taosheng Chen, Xiang Chen, Kevin W Freeman, Mark E Hatl